Canonical Allele Identifier: PA2741815214
Gene: GP1BB HGNC NCBI

Linked Data

ClinVar Variation Id: 2543665
ClinVar RCV Id: RCV004320616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000398.1:p.Ala184Asp
CA410677728
NM_000407.5:c.551C>A